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"Baiduoli" Renami heart rhythm system analyzer - Taiwan Registration ca5fef90062c42d8c6ddbb2894114e3e

Access comprehensive regulatory information for "Baiduoli" Renami heart rhythm system analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number ca5fef90062c42d8c6ddbb2894114e3e and manufactured by BIOTRONIC SE & CO. KG. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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ca5fef90062c42d8c6ddbb2894114e3e
Registration Details
Taiwan FDA Registration: ca5fef90062c42d8c6ddbb2894114e3e
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Device Details

"Baiduoli" Renami heart rhythm system analyzer
TW: โ€œ็™พๅคšๅŠ›โ€็‘ž่€ๅฝŒๅฟƒ่‡Ÿ็ฏ€ๅพ‹็ณป็ตฑๅˆ†ๆžๅ™จ
Risk Class 3

Registration Details

ca5fef90062c42d8c6ddbb2894114e3e

DHA05602565704

Company Information

Germany

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.3610 ๆคๅ…ฅๅผๅฟƒๅพ‹ๅ™จไน‹่„ˆๆ็”ข็”Ÿๅ™จ;; E.3630 ่„ˆๆ็”ข็”Ÿๅ™จไน‹ๅŠŸ่ƒฝๅˆ†ๆžๅ„€;; E.3600 ้ซ”ๅค–ๅผๅฟƒๅพ‹ๅ™จไน‹่„ˆๆ็”ข็”Ÿๅ™จ

import

Dates and Status

Dec 09, 2013

Dec 09, 2028